A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980817



Internal ID12982116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12300700..12581800hg38UCSC Ensembl
Innerchr9:12300700..12581800hg19UCSC Ensembl
Innerchr9:12290700..12571800hg18UCSC Ensembl
Innerchr9:12290700..12571800hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38281101
hg19281101
hg18281101
hg17281101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34901
Supporting Variants
SamplesNA19130
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980817
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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